课题组信息：
Ilija Čorić课题组隶属于苏黎世大学（UZH），该校成立于1833年，是瑞士最大的综合大学。苏黎世大学在分子生物学、神经科学、人类学等领域享有世界声誉，产生了爱因斯坦等12位诺贝尔奖得主。
研究方向
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fundamental transition metal chemistry with emphasis on multimetallic systems
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challenging reactions in organic synthesis and small molecule activation
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novel concepts and asymmetric methods for catalysis
招聘岗位：
Postdoc Position in Asymmetric Catalysis
Salary： ~7.7万瑞士法郎
The newly formed group at the University of Zurich performs research in the areas of organic and inorganic chemistry aiming at the development of advanced methods for homogeneous catalysis. We explore fundamental transition metal chemistry, as well as challenging reactions in organic synthesis and small molecule activation. Our goal is to advance the way molecules are made by enabling selective activation of strong chemical bonds in mild conditions. Specific areas of interest include: C-H activation, novel activation modes for catalysis, chemistry of multimetallic complexes, and design of chiral catalysts.
Applications that include cover letter, CV, brief research summary of previous work, transcripts of grades, and contact details of referees should be sent to: ilija.coric@chem.uzh.ch.
Ilija Čorić教授个人简介：
Ilija Čorić
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Group Leader, Department of Chemistry, University of Zurich, Switzerland, Sept. 2016-
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Postdoctoral Associate, Department of Chemistry, Yale University, USA, 2013-2016
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PhD, Max-Planck-Institut für Kohlenforschung, Mülheim/Ruhr, Germany, 2008-2012
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Medicinal Chemist, GlaxoSmithKline Research Centre Zagreb, Croatia, 2006-2008
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Diploma (M. Sc. Chemistry equivalent), University of Zagreb, Croatia, 2002-2006
代表性论文：
1). Insight into the Iron−Molybdenum Cofactor of Nitrogenase from Synthetic Iron Complexes with Sulfur, Carbon, and Hydride Ligands, Čorić, I.; Holland, P.L.* J. Am. Chem. Soc. 2016, 138, 7200.
2). Binding of dinitrogen to an iron–sulfur–carbon site, Čorić, I.; Mercado, B.Q.; Bill, E.; Vinyard, D.J.; Holland, P.L.*, Nature 2015, 526, 96.
3). The Catalytic Asymmetric α-Benzylation of Aldehydes, List, B.;* Čorić, I.; Grygorenko, O.O.; Kaib, P.S.J.; Komarov, I.; Lee, A.; Leutzsch, M.; Pan, S. C.; Tymtsunik, A. V.; van Gemmeren, M. Angew. Chem. Int. Ed. 2014, 53, 282.
4). Brønsted Acid Catalyzed Asymmetric SN2-Type O-Alkylations, Čorić, I.; Kim, J.H.; Vlaar, T.; Patil, M.; Thiel, W.; List, B.* Angew. Chem. Int. Ed. 2013, 52, 3490.
5). Asymmetric spiroacetalization catalysed by confined Brønsted acids, Čorić, I.; List, B.* Nature 2012, 483, 315.
6). Kinetic Resolution of Homoaldols via Catalytic Asymmetric Transacetalization, Čorić, I.;‡ Müller, S.;‡ List, B.* (‡Equal contribution), J. Am. Chem. Soc. 2010, 132, 17370.
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